The major sesquiterpene constituents of East-Indian sandalwood oil (Z)-α- and (Z)-β-santalols have shown to be responsible for most of the biological activities and organoleptic properties of sandalwood oil. The work reported here describes the strategic use of medium pressure liquid chromatography (MPLC) for the separation of both α- and β-santalenes and (Z)-α- and (Z)-β-santalols. Silver nitrate impregnated silica gel was used as the stationary phase in MPLC for quantitative separation of α- and β-santalenes and (Z)-α- and (Z)-β-santalols with mobile phases hexane and dichloromethane, respectively. The purities of α-santalene and (Z)-α-santalol obtained were >96%; however, β-santalene and (Z)-β-santalol were obtained with their respective inseparable epi-isomers. Limits of quantification (LoQ) relative to the FID detector were measured for important sesquiterpene alcohols of heartwood oil of S. album using serial dilutions of the standard stock solutions and demonstrated that the quality of the commercial sandalwood oil can be assessed for the content of individual sesquiterpene alcohols regulated by Australian Standard (AS2112-2003), International Organization for Standardization ISO 3518:2002 (E) and European Union (E. U.).
A simple and new colorimetric method was developed for the estimation of emtricitabine. The proposed colorimetric method is based on the diazotisation of amine group present in emtricitabine, followed by colour complex formation using β-naphthol reagent. Parameters affecting the reaction were studied and conditions were optimized. The absorption maximum for the colour complex was observed at 559 nm. Linearity was obtained in the concentration range of 100-500 µg/ml for emtricitabine colour complex. The developed method was optimised and validated. The method was successfully applied for the estimation of emtricitabine in bulk and in tablets. This is the first method reported for colorimetric estimation of emtricitabine.
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